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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303632Generated: November 1, 2026

Acetone → Tert-butyl 4-(iodomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2303632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium IodideHCID 5238—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
ProductTert-butyl 4-(iodomethyl)piperidine-1-carboxylateHCID 10448961—

Reaction Steps

A mixture of 1-(t-butoxycarbonyl)piperidin-4-yl methanesulfonate (13.58 g, 46.4 mmol) and sodium iodide (34.68 g, 232 mmol) in acetone (80 mL) was heated to reflux for 3 h. The mixture was partitioned between ether (350 mL) and water (350 mL). The organic layer was washed with saturated aq. brine (250 mL), and the aqueous layers were extracted in succession with ether (250 mL). The combined organic layers were dried (sodium sulfate), decanted, and evaporated to give the title compound (14.8 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-21a80cb2adc7424b85748a61b99513c8
Source noteuspto-grants-2002_08